What is NDC 37662-2863?

37662-2863 is the product NDC for Divalproex Sodium, Valproate sodium 12 [hp_C]/1 pellet, listed with the FDA by Hahnemann Laboratories, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Hahnemann Laboratories, INC., NDC labeler code 37662. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Divalproex Sodium?

184 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Divalproex Sodium NDC 37662-2863 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-2863Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-2863Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
37662-2863-1	37662286301	200 PELLET in 1 VIAL, GLASS (37662-2863-1)Marketed from Mar 28, 2023
37662-2863-2	37662286302	1200 PELLET in 1 BOTTLE, GLASS (37662-2863-2)Marketed from Mar 28, 2023
37662-2863-3	37662286303	4000 PELLET in 1 BOTTLE, GLASS (37662-2863-3)Marketed from Mar 28, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Divalproex Sodium
Generic name (nonproprietary): divalproex sodium
Active ingredients: Valproate sodium — 12 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, INC.NDC labeler code 37662
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 28, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 37662-2863_f7fec516-ec70-6248-e053-6294a90a3342SPL ID f7fec516-ec70-6248-e053-6294a90a3342SPL set ID f7fec516-ec6f-6248-e053-6294a90a3342UNII 5VOM6GYJ0D
Pharmacologic class: Anti-epileptic Agent; Mood Stabilizer

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N437662286301 followed by a unit qualifier and the quantity

Package 37662-2863-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 28, 2023.

Full label on DailyMed (opens in a new tab)

About NDC 37662-2863

What is NDC 37662-2863?: 37662-2863 is the product NDC for Divalproex Sodium, Valproate sodium 12 [hp_C]/1 pellet, listed with the FDA by Hahnemann Laboratories, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Divalproex Sodium.
What is the active ingredient?: Valproate sodium.
Who is the labeler?: Hahnemann Laboratories, INC., NDC labeler code 37662. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Divalproex Sodium?: 184 other product NDCs are listed under this name. See all Divalproex Sodium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Divalproex Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-4193	68788-4193-0368788-4193-0668788-4193-09
divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-1683	67046-1683-03
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-028	87441-0028-01
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-027	87441-0027-01
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-2021	67046-2021-03
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-4100	68788-4100-0368788-4100-0668788-4100-09
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Safecor Health, LLC	48433-033	48433-0033-08
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Safecor Health, LLC	48433-034	48433-0034-08
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-4575	70518-4575-00
divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-4079	68788-4079-0368788-4079-0668788-4079-09

All 185 Divalproex Sodium NDCs